Canonical Allele Identifier: PA891849738
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 582573
ClinVar RCV Id: RCV000706680 RCV001775979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Trp93Ser
CA411090405
NM_007194.4:c.278G>C